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L WEMEAU

Showing results (71-80 of 85) with videos related to

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Gynecologie, Obstetrique & Fertilite|March 9, 2005
[Small cell carcinoma of the ovary of the hypercalcemic type revealed by a severe acute pancreatitis: about one case]A Bourgain, O Acker, E Lambaudie, et al.
Annales De Chirurgie|December 21, 2002
[Prospective study of early predictive factors of permanent hypocalcemia after bilateral thyroidectomy]M Jafari, F Pattou, B Soudan, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Journal of Nuclear Biology and Medicine (Turin, Italy : 1991)|October 1, 1991
Treatment of malignant pheochromocytoma with [131I]metaiodobenzylguanidine: a French multicenter studyM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1991
Use of m-[131I]iodobenzylguanidine in the treatment of malignant pheochromocytomaM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinomaP Pigny, C Bauters, J L Wemeau, et al.
Clinical Endocrinology|March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Clinical Endocrinology|May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismM C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Annales De Chirurgie|March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]A Lamblin, P Pigny, G Tex, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Gynecologie, Obstetrique & Fertilite|March 9, 2005
[Small cell carcinoma of the ovary of the hypercalcemic type revealed by a severe acute pancreatitis: about one case]A Bourgain, O Acker, E Lambaudie, et al.
Annales De Chirurgie|December 21, 2002
[Prospective study of early predictive factors of permanent hypocalcemia after bilateral thyroidectomy]M Jafari, F Pattou, B Soudan, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Journal of Nuclear Biology and Medicine (Turin, Italy : 1991)|October 1, 1991
Treatment of malignant pheochromocytoma with [131I]metaiodobenzylguanidine: a French multicenter studyM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1991
Use of m-[131I]iodobenzylguanidine in the treatment of malignant pheochromocytomaM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinomaP Pigny, C Bauters, J L Wemeau, et al.
Clinical Endocrinology|March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Clinical Endocrinology|May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismM C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Annales De Chirurgie|March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]A Lamblin, P Pigny, G Tex, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Pageof 9